Kathrin Siepermann
Krefeld, NW 47805, Germany
Last Updated: 09/26/2026
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Found 8 publications
UNC93B1 variants underlie TLR7-dependent autoimmunity.
Journal: Science immunology
Published: January 11, 2024
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50.
Journal: Frontiers in immunology
Published: June 09, 2022
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome.
Journal: European journal of immunology
Published: December 06, 2019
Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome.
Journal: Haematologica
Published: October 30, 2016
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency.
Journal: The Journal of allergy and clinical immunology
Published: August 27, 2014
Successful HLA haploidentical hematopoietic SCT in chronic granulomatous disease.
Journal: Bone marrow transplantation
Published: June 24, 2014
Challenges of genetic counseling in patients with autosomal dominant diseases, such as the hyper-IgE syndrome (STAT3-HIES).
Journal: The Journal of allergy and clinical immunology
Published: June 18, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026